6 positions on this site are linked to Cardiovascular Disease Risk Factors, out of 24,209 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
SLC17A4 · rs11754288
See detailed info → SensitivePCSK7 · rs508487
See detailed info → SensitiveAPOB · rs10199768
See detailed info → SensitiveLPL · rs17091905
See detailed info → SensitiveBCHE · rs1803274
See detailed info → Sensitivenear ZNF518B · rs4698036
See detailed info →One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.
The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.
No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.
Yes — the search box above matches gene symbols and rsIDs as well as trait names.